Mike Gerards

Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected by the Mitochondrial DNA–Haplogroup Background

Gavin Hudson, Valério Carelli, Liesbeth Spruijt et al. · The American Journal of Human Genetics · 2007 · 356 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene

Mike Gerards, B.J.C. van den Bosch, Katharina Danhauser et al. · Brain · 2010 · 128 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause

Tom E. J. Theunissen, Minh Nguyen, Rick Kamps et al. · Frontiers in Genetics · 2018 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Exome sequencing reveals a novel Moroccan founder mutation in<i>SLC19A3</i>as a new cause of early-childhood fatal Leigh syndrome

Mike Gerards, Rick Kamps, Jo van Oevelen et al. · Brain · 2013 · 95 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A hitchhiker’s guide to mitochondrial quantification

Irene M. G. M. Hemel, Bob P. H. Engelen, Nicole Luber et al. · Mitochondrion · 2021 · 75 citations · Full text

Life Sciences, Bioinformatics, Biology +12